Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA).
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity.
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Manufacturer's By Device Corneal bur manual instrument-Corneal bur manual instrument
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Manufacturer
Address
Authorised Representative
Address
Date Registered
MHRA Reference Number
Bausch & Lomb GmbH
Im Schuhmachergewann 4
Heidelberg
D-69123
Germany
Bausch & Lomb U.K. Ltd.
106-114 London Road
Kingston upon Thames
Surrey KT2 6TN
England United Kingdom
07/14/2021
15805